NMDP-02 is under clinical development by NMD Pharma and currently in Phase II for Spinal Muscular Atrophy (SMA). According to GlobalData, Phase II drugs for Spinal Muscular Atrophy (SMA) have a 71% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how NMDP-02’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.

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GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

NMDP-02 overview

NMDP-02 is under development for the treatment of spinal muscular atrophy type 3. It acts by targeting chloride channel protein 1 (CLC-1). It is administered through oral route in the form of tablets.

See Also:

NMD Pharma overview

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NMD Pharma discovers and develops novel therapeutics for neuromuscular diseases. It develops novel treatments that strengthen neuromuscular transmission and muscle function. NMD Pharma product pipeline includes NMDP-01 (NMD670), NMDP-02 (NMD670),NMDP-03 (NMD1343),NMDP-04, NMDP-05 and NMDP-06. Its product pipeline treats myasthenia gravis, spinal muscular atrophy, rare neuromuscular disease, scarcopenia and reversal of neuromuscular block. The company carries out translational muscle electrophysiology platform. It also utilizing ClC-1 Cl- ion channel inhibitors for neuromuscular diseases. NMD Pharma is headquartered in Aarhus, Denmark.

For a complete picture of NMDP-02’s drug-specific PTSR and LoA scores, buy the report here.